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Journal of Luminescence
journal homepage: www.elsevier.com/locate/jlumin
A B S T R A C T
Silver nanoparticles (AgNPs) present unique physical and chemical properties such as chemical stability, huge
superficial area and excellent optical properties, thus justifying the impact and variety of their applications: in
material science, in electrochemistry, in electronic devices, as biological or chemical sensors, and in catalysis.
Given the fact that there is a limited number of studies on synthesis of AgNPs compared with other
nanomaterials, this article proposes a simple methodology for synthesizing AgNPs involving the wet chemical
reduction of silver nitrate with gallic acid as a reduction/capping reagent. The reaction is carried out in absence
or in presence of hydrogen peroxide; and the formation of AgNPs is monitored by UV–vis and fluorescence
spectroscopy. Transmission electron microscopy (TEM), atomic force microscopy (AFM), and X-ray photoelec-
tron spectroscopy (XPS) were used for further characterization. Two main types of nanoparticles/nanodiscs were
clearly identified in absence and in presence of hydrogen peroxide, respectively. Thus, AFM revealed the
formation of AgNPs of 18.15 ± 1.95 nm in diameter and of 2.21 ± 0.35 nm high or of 9.16 ± 1.28 nm in
diameter and of 1.57 ± 0.17 nm high. The STM technique revealed that average particle size was
4.59 ± 0.61 nm with hydrogen peroxide and 3.84 ± 0.66 nm without it. Therefore, the nanoparticle size
obtained by AFM was strongly influenced by the capping thickness. The reduction in nanoparticle size was
accompanied by increased uniformity and reproducibility. The fluorescence of the AgNPs was used to determine
traces of iron in tap water and bottled water via an induced fluorescence quenching mechanism, thus aiding in
establishing an analytical method.
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Corresponding author.
E-mail address: fjimenez@ull.edu.es (F. Jiménez-Moreno).
http://dx.doi.org/10.1016/j.jlumin.2017.05.052
Received 31 May 2016; Received in revised form 17 May 2017; Accepted 20 May 2017
Available online 22 May 2017
0022-2313/ © 2017 Elsevier B.V. All rights reserved.